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The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC)
This study is currently recruiting participants.
Study NCT00605072   Information provided by National Institute on Aging (NIA)
First Received: January 11, 2008   Last Updated: September 9, 2009   History of Changes

January 11, 2008
September 9, 2009
January 2008
December 2011   (final data collection date for primary outcome measure)
Cognitive assessment measured by Trail Making Test, Hopkins Verbal Learning Test - Revised (HVLT-R), and Digit Span Test [ Time Frame: Baseline, 1, 6, and 12 months ] [ Designated as safety issue: No ]
Cognitive assessment measured by Trail Making Test, Hopkins Verbal Learning Test - Revised (HVLT-R), and Digit Span Test [ Time Frame: Baseline, 1 and 6 months ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00605072 on ClinicalTrials.gov Archive Site
  • Changes in Cerebral Blood Flow (CBF) and cerebral vasoreactivity [ Time Frame: Baseline, then 6 and 12 months after BP control ] [ Designated as safety issue: No ]
  • Endothelial function assessed using the flow mediated dilatation (FMD) procedure [ Time Frame: Baseline, then 6 and 12 months after BP control ] [ Designated as safety issue: No ]
  • Biochemical measurement to monitor for adverse events: hyperkalemia, renal failure, leukopenia and liver function abnormalities [ Time Frame: Baseline, 2-4 weeks, 2, 4, 9, and 12 months ] [ Designated as safety issue: Yes ]
  • Changes in Cerebral Blood Flow (CBF) and cerebral vasoreactivity [ Time Frame: Baseline, and 6 months after BP control ] [ Designated as safety issue: No ]
  • Endothelial function assessed using the flow mediated dilatation (FMD) procedure [ Time Frame: Baseline, and 6 months after BP control ] [ Designated as safety issue: No ]
  • Biochemical measurement to monitor for adverse events: hyperkalemia, renal failure, leukopenia and liver function abnormalities [ Time Frame: Baseline, 2-4 weeks, 2, 4, and 9 months ] [ Designated as safety issue: Yes ]
 
The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial
The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC Trial)

The purpose of this study is to examine the effects of blood pressure medications on cognition and blood flow in hypertensive elderly patients with cognitive impairment. The hypothesis is that treatment with an angiotensin receptor blocker (ARB) or an angiotensin-converting enzyme inhibitor (ACEI) will be associated with a slower rate of further cognitive decline, improved cerebral blood flow and its regulation, and preserved physical function as compared to treatment with a diuretic (HCTZ), independent of blood pressure level.

There is mounting evidence that hypertension, which affects more than 65% of the US elderly population, accelerates cognitive decline and increases the risk of functional disability among older individuals. Hypertension is also associated with cerebral blood flow reduction and dysregulation which contribute to further cognitive and functional impairment. Drugs that inhibit angiotensin II (ACEI and ARB) are commonly used antihypertensives and may have a protective effect on cognitive function, cerebral blood flow and physical function compared to other antihypertensives such as hydrochlorothiazide (HCTZ).

A total of 100 individuals will be recruited for this pilot 3-arm randomized study to investigate the effects of: (i) 12 months treatment with candesartan (ARB) compared to hydrochlorothiazide (HCTZ) and (ii) 12 months treatment with lisinopril (ACEI) compared to HCTZ and (iii) to estimate the effect size difference between lisinopril and losartan on cognition, cerebral blood flow regulation, and functional measures in a sample of elderly hypertensive individuals with objective evidence of cognitive impairment.

Phase II
Interventional
Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Efficacy Study
  • Cognitive Impairment
  • Hypertension
  • Aging
  • Drug: candesartan
  • Drug: lisinopril
  • Drug: hydrochlorothiazide
  • Drug: nifedipine, long acting
  • Drug: metoprolol, long-acting
  • Experimental: Angiotensin Receptor Blocker
  • Experimental: Angiotensin-Converting Enzyme (ACE) Inhibitor

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
100
December 2011
December 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 60 years or older
  • Hypertension
  • Cognitive criteria: score either 10 or less out of 15 for the executive clock draw test 1 (CLOX1) or less than or equal to 1 standard deviation from the corresponding age specific mean on the immediate memory subtest

Exclusion Criteria:

  • Intolerance to ACEI or ARB
  • History of congestive heart failure
  • History of diabetes mellitus
  • History of stroke (less than 6 months)
Both
60 Years and older
No
Contact: Meaghan Hart 617-363-8484 MeaghanHart@hrca.harvard.edu
United States
 
NCT00605072
Ihab Hajjar, MD, Hebrew SeniorLife
IA0127, 1K23AG30057-01A1
National Institute on Aging (NIA)
Hebrew SeniorLife
Principal Investigator: Ihab Hajjar, MD Hebrew SeniorLife
National Institute on Aging (NIA)
September 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP